Venables Samantha J, Mehta Bhavik, Daniel Runa, Walsh Simon J, van Oorschot Roland A H, McNevin Dennis
National Centre for Forensic Studies, Faculty of Education, Science, Technology and Mathematics, University of Canberra, Canberra, Australia.
Electrophoresis. 2014 Nov;35(21-22):3036-43. doi: 10.1002/elps.201400089. Epub 2014 Oct 1.
High resolution melting (HRM) analysis is a simple, cost effective, closed tube SNP genotyping technique with high throughput potential. The effectiveness of HRM for forensic SNP genotyping was assessed with five commercially available HRM kits evaluated on the ViiA™ 7 Real Time PCR instrument. Four kits performed satisfactorily against forensically relevant criteria. One was further assessed to determine the sensitivity, reproducibility, and accuracy of HRM SNP genotyping. The manufacturer's protocol using 0.5 ng input DNA and 45 PCR cycles produced accurate and reproducible results for 17 of the 19 SNPs examined. Problematic SNPs had GC rich flanking regions which introduced additional melting domains into the melting curve (rs1800407) or included homozygotes that were difficult to distinguish reliably (rs16891982; a G to C SNP). A proof of concept multiplexing experiment revealed that multiplexing a small number of SNPs may be possible after further investigation. HRM enables genotyping of a number of SNPs in a large number of samples without extensive optimization. However, it requires more genomic DNA as template in comparison to SNaPshot®. Furthermore, suitably modifying pre-existing forensic intelligence SNP panels for HRM analysis may pose difficulties due to the properties of some SNPs.
高分辨率熔解(HRM)分析是一种简单、经济高效的闭管单核苷酸多态性(SNP)基因分型技术,具有高通量潜力。使用在ViiA™ 7实时荧光定量PCR仪上评估的五种市售HRM试剂盒,对HRM用于法医SNP基因分型的有效性进行了评估。四种试剂盒在法医相关标准方面表现令人满意。对其中一种试剂盒进行了进一步评估,以确定HRM SNP基因分型的灵敏度、重复性和准确性。使用制造商的方案,以0.5 ng输入DNA和45个PCR循环,对所检测的19个SNP中的17个产生了准确且可重复的结果。有问题的SNP具有富含GC的侧翼区域,这会在熔解曲线中引入额外的熔解结构域(rs1800407),或者包含难以可靠区分的纯合子(rs16891982;一个从G到C的SNP)。一项概念验证多重实验表明,经过进一步研究,少量SNP的多重分析可能是可行的。HRM能够在大量样本中对多个SNP进行基因分型,而无需进行广泛优化。然而,与SNaPshot®相比,它需要更多的基因组DNA作为模板。此外,由于某些SNP的特性,对预先存在的法医情报SNP面板进行适当修改以用于HRM分析可能会遇到困难。